Canonical Allele Identifier: PA2828318975
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 737525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Ala1328Val
CA43734177
NM_001369346.1:c.3983C>T